This webinar will offer a thorough understanding of the preclinical testing requirements outlined in Regulation (EU) 2017/745 on medical devices. In collaboration with TUV SUD, a leading notified body, participants will gain direct access to expert knowledge essential for regulatory compliance.
What’s on the programme:
- Uncover the detailed preclinical testing requirements as stipulated by Regulation (EU) 2017/745 for medical devices.
- Benefit from the expertise of TUV SUD professionals and gain practical insights into achieving regulatory compliance.
- Evaluate the significance of preclinical testing in confirming the safety and functionality of medical devices.
- Join interactive Q&A segments to resolve any uncertainties and enhance your grasp of regulatory demands.
Registrations are now open! Reserve your spot here: WEBINAR REGISTRATION
Speakers: Carlo Gherardi (TÜV SÜD) and Patricia Marmol (Asphalion)
Need expert support with your Medical Devices development or regulatory strategy? Contact us at: [email protected]
